Congenital exomphalos

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL EXOMPHALOS
C1306503
CHRNA7 Unknown — Disgenet
PCSK5 Unknown — Disgenet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital exomphalos.
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15q13.3 microdeletion syndrome 1 shared geneCHRNA7 Related via 1 shared gene including CHRNA7. Auditory perceptual disorder 1 shared geneCHRNA7 Related via 1 shared gene including CHRNA7. Congenital omphalocele 2 shared genesCHRNA7, PCSK5 Related via 2 shared genes including CHRNA7, PCSK5. Currarino syndrome 1 shared genePCSK5 Related via 1 shared gene including PCSK5. Sacral defect 1 shared genePCSK5 Related via 1 shared gene including PCSK5.